TY - JOUR
T1 - Cutaneous chronic graft versus host disease following allogeneic haematopoietic stem cell transplantation in children
T2 - A retrospective study
AU - Shreberk-Hassidim, Rony
AU - Neumark, Michal
AU - Greenberger, Shoshana
AU - Goldstein, Gal
AU - Hassidim, Ayal
AU - Dukler, Yuval
AU - Maly, Alexander
AU - Stepensky, Polina
AU - Molho-Pessach, Vered
N1 - Publisher Copyright:
© 2018 Acta Dermato-Venereologica.
PY - 2018/2
Y1 - 2018/2
N2 - Chronic graft versus host disease (cGVHD) is a complication of allogeneic haematopoietic stem cell transplantation (HSCT). The aim of this study was to clinically characterize childhood cutaneous cGVHD. A retrospective study of children treated with HSCT at 2 tertiary medical centres in Israel between 2011 and 2014 was performed. A total of 112 children were included. Cutaneous cGVHD developed in 18% of subjects. Risk factors were older age, HSCT from peripheral blood and acute lymphoblastic leukaemia. The eruption was lichenoid in 90% of subjects, of whom one-third progressed to sclerosis. Topical treatments were usually sufficient in localized disease. Widespread eruption necessitated phototherapy, extracorporeal photopheresis and/or systemic immunosuppressants. Patients presenting with palmoplantar keratoderma, developed sclerosis. To the best of our knowledge, this is the first study describing childhood cutaneous cGV-HD. Lichenoid eruption is the most common cutaneous pattern of cGVHD in children. Sclerotic changes may be associated with prior keratoderma. cGVHD poses a therapeutic challenge and better treatments should be sought.
AB - Chronic graft versus host disease (cGVHD) is a complication of allogeneic haematopoietic stem cell transplantation (HSCT). The aim of this study was to clinically characterize childhood cutaneous cGVHD. A retrospective study of children treated with HSCT at 2 tertiary medical centres in Israel between 2011 and 2014 was performed. A total of 112 children were included. Cutaneous cGVHD developed in 18% of subjects. Risk factors were older age, HSCT from peripheral blood and acute lymphoblastic leukaemia. The eruption was lichenoid in 90% of subjects, of whom one-third progressed to sclerosis. Topical treatments were usually sufficient in localized disease. Widespread eruption necessitated phototherapy, extracorporeal photopheresis and/or systemic immunosuppressants. Patients presenting with palmoplantar keratoderma, developed sclerosis. To the best of our knowledge, this is the first study describing childhood cutaneous cGV-HD. Lichenoid eruption is the most common cutaneous pattern of cGVHD in children. Sclerotic changes may be associated with prior keratoderma. cGVHD poses a therapeutic challenge and better treatments should be sought.
KW - Allogeneic haematopoietic cell transplantation
KW - Children
KW - Chronic cutaneous graft versus host disease
KW - Graft versus host disease
KW - Lichenoid
KW - Sclerotic
UR - http://www.scopus.com/inward/record.url?scp=85041284455&partnerID=8YFLogxK
U2 - 10.2340/00015555-2824
DO - 10.2340/00015555-2824
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C2 - 29057425
AN - SCOPUS:85041284455
VL - 98
SP - 206
EP - 211
JO - Acta Dermato-Venereologica
JF - Acta Dermato-Venereologica
SN - 0001-5555
IS - 2
ER -